Job summary
Job post source
This job is directly from Worldwide Clinical Trials
Job overview
The Senior Medical Writer role at Worldwide Clinical Trials involves leading medical writing teams to prepare regulatory and clinical study documents, impacting the quality and compliance of clinical trial communications globally.
Responsibilities and impact
The role requires preparing and leading the creation of Phase I-IV study documents, collaborating with various departments on regulatory submissions, managing document templates, and serving as a publishing contact for clinical trial reports.
Compensation and benefits
The salary range is $80,735 to $160,265, with compensation varying by skills, experience, and location; benefits details are not specified.
Experience and skills
Candidates need a life science degree or equivalent, at least 4 years of medical writing experience, excellent English, strong project management, Microsoft Office proficiency, and knowledge of regulatory guidelines like ICH E3, E6, and E9; travel availability is required.
Career development
The company offers ongoing training and career development opportunities within a dynamic global medical writing team.
Work environment and culture
Worldwide Clinical Trials promotes a diverse, inclusive, and collaborative culture with accessible leadership and supportive teams, encouraging employees to thrive and do their best work.
Company information
Worldwide Clinical Trials is a global midsize CRO with over 3,500 employees, focused on innovative clinical research to improve patient lives worldwide.
Team overview
The medical writing team is global, dynamic, and supported by leadership and peers, working closely with subject matter experts and regulatory strategists.
Job location and travel
This is a remote position available in the UK and US, with domestic and international travel required.
Unique job features
The role involves working on a wide range of therapeutic areas and regulatory regions, with opportunities to lead teams and manage key document templates, distinguishing it from similar roles.
Company overview
Worldwide Clinical Trials is a global contract research organization (CRO) that provides phase I-IV clinical trial services to the pharmaceutical and biotechnology industries. They specialize in therapeutic areas such as neuroscience, cardiovascular, metabolic, and rare diseases. Founded in 1986, the company has grown to operate in more than 60 countries, leveraging their scientific expertise and innovative technologies to deliver high-quality data and support drug development. Their revenue is primarily generated through service contracts with pharmaceutical companies, offering comprehensive clinical trial management, data analysis, and regulatory support.
How to land this job
Position your resume to highlight your expertise in medical writing for Phase I-IV clinical study documents, emphasizing your ability to lead teams and manage complex regulatory submissions across multiple regions including the USA, Europe, and ROW.
Focus on showcasing your proficiency with regulatory guidelines such as ICH E3, E6, and E9, your strong command of English, and your experience managing document templates and publishing processes in compliance with global standards.
Apply through multiple platforms including Worldwide Clinical Trials’ official corporate careers page, LinkedIn job postings, and other reputable job boards where the Senior Medical Writer role is listed to maximize your application visibility.
Connect with current medical writers, regulatory strategists, or clinical methodologists at Worldwide Clinical Trials on LinkedIn; open your messages with ice breakers like referencing a recent Worldwide Clinical Trials publication, asking about their experience with cross-regional regulatory challenges, or expressing enthusiasm for their innovation-driven culture.
Optimize your resume for ATS by incorporating keywords from the job description such as 'medical writing,' 'Phase I-IV clinical trials,' 'ICH guidelines,' 'protocol development,' 'regulatory submissions,' and 'document management' to ensure your resume passes initial automated screenings.
Utilize Jennie Johnson's Power Apply feature to automate the tailoring of your resume, identify multiple application channels, and find relevant LinkedIn contacts to network with, freeing up your time to focus on preparing for interviews and other job search activities.
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